M. Momtchilova

Early-onset Behr syndrome due to compound heterozygous mutations in OPA1.

V. Desquiret-Dumas, E. Colin, D. Bonneau, 2014, Brain : a journal of neurology.

Amblyopia and peri-ocular capillary hemangioma of infancy : screening and prossession before and after surgery

M. Vazquez, M. Momtchilova, L. Laroche, 2004 .

[Congenital Horner syndrome associated with hypoplasia of the internal carotid artery].

H. Ducou le Pointe, M. Momtchilova, L. Laroche, 2009, Journal francais d'ophtalmologie.

Retinal involvement in two unrelated patients with Myhre syndrome.

A. Afenjar, N. Dorison, J. Le Gargasson, 2012, European journal of medical genetics.

Use of ultrasonic dissection in the early surgical management of periorbital haemangiomas.

M. Vazquez, M. Momtchilova, A. Picard, 2008, Journal of plastic, reconstructive & aesthetic surgery : JPRAS.

[Susac syndrome and ocular manifestation in a 14-year-old girl].

M. Momtchilova, L. Laroche, B. Pelosse, 2007, Journal francais d'ophtalmologie.

Novel mutation in SLC9A6 gene in a patient with Christianson syndrome and retinitis pigmentosum

M. Momtchilova, D. Heron, C. Mignot, 2013, Brain and Development.

[Kikuchi's disease and ocular manifestation].

F. Rocher, M. Momtchilova, L. Laroche, 2006, Journal francais d'ophtalmologie.

[Congenital Horner syndrome associated with hypoplasia of the internal carotid artery].

M. Momtchilova, L. Laroche, M. Balu, 2009, Journal francais d'ophtalmologie.